@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_head {
  this: np:hasAssertion dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_assertion ;
    np:hasProvenance dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_provenance ;
    np:hasPublicationInfo dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_assertion a np:Assertion .
  dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_provenance a np:Provenance .
  dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_assertion {
  miriam-gene:6352 a ncit:C16612 .
  lld:C0039103 a ncit:C7057 .
  dgn-gda:DGN56f02cc9fc93bb02be78a391686b7628 sio:SIO_000628 miriam-gene:6352 , lld:C0039103 ;
    a sio:SIO_001121 .
}
dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_provenance {
  dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_assertion dcterms:description "[No significant differences were observed between the patients carrying the CCR5 delta 32 allele and those homozygous for the normal CCR5 allele when we compared sex, presence of distal synovitis and systemic signs and/or symptoms, initial and cumulative prednisone dose, duration of therapy, ESR at diagnosis, frequency of relapse/recurrence and RANTES serum levels at diagnosis and after 6 months of corticosteroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:11072599 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP388703.RAF6vVB4U4wD7O6QPhLT1Uw-JHcOhsHT0wnM0z-EADYDg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}